Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930426L09Rik |
T |
C |
2: 19,003,623 (GRCm39) |
|
probably benign |
Het |
Abi3bp |
A |
G |
16: 56,462,930 (GRCm39) |
|
probably benign |
Het |
Asb4 |
T |
C |
6: 5,398,386 (GRCm39) |
I117T |
probably benign |
Het |
Birc6 |
T |
G |
17: 74,946,822 (GRCm39) |
L2847R |
probably damaging |
Het |
C2cd2 |
A |
G |
16: 97,691,208 (GRCm39) |
|
probably benign |
Het |
Ccdc77 |
C |
A |
6: 120,316,119 (GRCm39) |
C186F |
possibly damaging |
Het |
Cd300ld2 |
T |
A |
11: 114,903,384 (GRCm39) |
|
probably benign |
Het |
Cd55b |
A |
T |
1: 130,345,919 (GRCm39) |
D166E |
probably benign |
Het |
Cfap100 |
A |
G |
6: 90,390,954 (GRCm39) |
F8L |
probably damaging |
Het |
Col2a1 |
C |
T |
15: 97,884,618 (GRCm39) |
|
probably null |
Het |
Dbf4 |
A |
G |
5: 8,453,189 (GRCm39) |
I270T |
probably benign |
Het |
Dkk3 |
T |
C |
7: 111,748,236 (GRCm39) |
S123G |
probably benign |
Het |
Ep400 |
A |
G |
5: 110,824,809 (GRCm39) |
|
probably benign |
Het |
Fam184a |
A |
G |
10: 53,575,351 (GRCm39) |
I30T |
probably damaging |
Het |
Fam20a |
T |
C |
11: 109,564,239 (GRCm39) |
I505V |
probably benign |
Het |
Fbh1 |
T |
C |
2: 11,768,938 (GRCm39) |
D285G |
probably benign |
Het |
Fcho1 |
T |
C |
8: 72,169,444 (GRCm39) |
E154G |
probably damaging |
Het |
Klhdc1 |
A |
G |
12: 69,329,958 (GRCm39) |
I362M |
probably benign |
Het |
Knl1 |
A |
T |
2: 118,931,255 (GRCm39) |
E1990D |
probably benign |
Het |
Lancl2 |
A |
G |
6: 57,711,024 (GRCm39) |
Y394C |
probably damaging |
Het |
Map2k7 |
A |
G |
8: 4,288,950 (GRCm39) |
E14G |
probably damaging |
Het |
Mga |
A |
G |
2: 119,754,517 (GRCm39) |
I1009V |
probably damaging |
Het |
Nat9 |
C |
A |
11: 115,074,234 (GRCm39) |
|
probably null |
Het |
Nek2 |
G |
A |
1: 191,563,401 (GRCm39) |
A422T |
probably benign |
Het |
Nfkbiz |
A |
T |
16: 55,636,034 (GRCm39) |
L509Q |
probably damaging |
Het |
Or56b2 |
A |
T |
7: 104,337,634 (GRCm39) |
R137S |
probably benign |
Het |
Pgap1 |
T |
A |
1: 54,587,147 (GRCm39) |
Q143L |
probably damaging |
Het |
Pkd1l3 |
C |
T |
8: 110,392,217 (GRCm39) |
T1937I |
probably damaging |
Het |
Pou1f1 |
A |
G |
16: 65,326,784 (GRCm39) |
E128G |
probably damaging |
Het |
Ppfia3 |
T |
C |
7: 44,989,996 (GRCm39) |
|
probably benign |
Het |
Prkd1 |
T |
C |
12: 50,434,046 (GRCm39) |
I566V |
probably benign |
Het |
Psd2 |
A |
G |
18: 36,138,959 (GRCm39) |
R528G |
probably damaging |
Het |
Ptprg |
G |
T |
14: 12,110,080 (GRCm38) |
E263* |
probably null |
Het |
Radil |
T |
C |
5: 142,529,576 (GRCm39) |
D40G |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,750,442 (GRCm39) |
Y1943F |
probably damaging |
Het |
Slc30a4 |
C |
T |
2: 122,543,947 (GRCm39) |
|
probably benign |
Het |
Slc31a1 |
A |
T |
4: 62,306,241 (GRCm39) |
T120S |
possibly damaging |
Het |
Snrpe |
A |
G |
1: 133,537,487 (GRCm39) |
|
probably benign |
Het |
Stx3 |
G |
T |
19: 11,796,046 (GRCm39) |
|
probably benign |
Het |
Thoc2l |
A |
G |
5: 104,666,867 (GRCm39) |
E463G |
possibly damaging |
Het |
Ufsp1 |
T |
A |
5: 137,293,178 (GRCm39) |
C43S |
probably damaging |
Het |
Vac14 |
T |
A |
8: 111,379,950 (GRCm39) |
M416K |
possibly damaging |
Het |
Vmn1r81 |
A |
C |
7: 11,993,792 (GRCm39) |
V272G |
possibly damaging |
Het |
Vmn2r107 |
T |
A |
17: 20,578,062 (GRCm39) |
I457K |
probably benign |
Het |
Vmn2r72 |
A |
T |
7: 85,387,374 (GRCm39) |
V730E |
probably benign |
Het |
Vmn2r9 |
T |
C |
5: 108,995,433 (GRCm39) |
Y405C |
probably damaging |
Het |
Zcchc17 |
T |
C |
4: 130,210,440 (GRCm39) |
*242W |
probably null |
Het |
Zfp503 |
T |
C |
14: 22,037,354 (GRCm39) |
K83R |
possibly damaging |
Het |
|
Other mutations in Lgi2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00861:Lgi2
|
APN |
5 |
52,695,463 (GRCm39) |
missense |
probably benign |
|
IGL01310:Lgi2
|
APN |
5 |
52,711,807 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03091:Lgi2
|
APN |
5 |
52,721,307 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03367:Lgi2
|
APN |
5 |
52,719,502 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03388:Lgi2
|
APN |
5 |
52,695,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R0388:Lgi2
|
UTSW |
5 |
52,711,891 (GRCm39) |
missense |
probably damaging |
0.99 |
R0602:Lgi2
|
UTSW |
5 |
52,711,765 (GRCm39) |
missense |
probably damaging |
0.98 |
R0633:Lgi2
|
UTSW |
5 |
52,711,802 (GRCm39) |
missense |
probably damaging |
0.97 |
R1616:Lgi2
|
UTSW |
5 |
52,703,980 (GRCm39) |
missense |
probably benign |
0.00 |
R1916:Lgi2
|
UTSW |
5 |
52,703,974 (GRCm39) |
missense |
probably benign |
|
R2072:Lgi2
|
UTSW |
5 |
52,695,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R2512:Lgi2
|
UTSW |
5 |
52,695,307 (GRCm39) |
makesense |
probably null |
|
R4614:Lgi2
|
UTSW |
5 |
52,695,775 (GRCm39) |
missense |
probably damaging |
0.99 |
R4855:Lgi2
|
UTSW |
5 |
52,695,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R5092:Lgi2
|
UTSW |
5 |
52,695,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R5181:Lgi2
|
UTSW |
5 |
52,711,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R5311:Lgi2
|
UTSW |
5 |
52,711,827 (GRCm39) |
missense |
probably damaging |
0.99 |
R6074:Lgi2
|
UTSW |
5 |
52,703,984 (GRCm39) |
missense |
probably benign |
|
R7089:Lgi2
|
UTSW |
5 |
52,695,832 (GRCm39) |
missense |
probably damaging |
0.99 |
R7376:Lgi2
|
UTSW |
5 |
52,695,604 (GRCm39) |
missense |
probably damaging |
0.99 |
R7396:Lgi2
|
UTSW |
5 |
52,695,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R7733:Lgi2
|
UTSW |
5 |
52,695,873 (GRCm39) |
missense |
probably benign |
0.03 |
R8007:Lgi2
|
UTSW |
5 |
52,723,375 (GRCm39) |
missense |
probably benign |
0.01 |
R8073:Lgi2
|
UTSW |
5 |
52,704,013 (GRCm39) |
missense |
probably benign |
|
R9137:Lgi2
|
UTSW |
5 |
52,695,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R9484:Lgi2
|
UTSW |
5 |
52,695,936 (GRCm39) |
missense |
probably benign |
0.36 |
R9505:Lgi2
|
UTSW |
5 |
52,711,775 (GRCm39) |
missense |
probably benign |
0.00 |
R9723:Lgi2
|
UTSW |
5 |
52,695,843 (GRCm39) |
missense |
probably damaging |
1.00 |
|